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Campo DCValorIdioma
dc.contributor.authorCarvalho, P. P.-
dc.contributor.authorLeonor, I. B.-
dc.contributor.authorSmith, Brenda J.-
dc.contributor.authorDias, Isabel R.-
dc.contributor.authorReis, R. L.-
dc.contributor.authorGimble, Jeffrey M.-
dc.contributor.authorGomes, Manuela E.-
dc.date.accessioned2013-12-11T16:33:14Z-
dc.date.available2013-12-11T16:33:14Z-
dc.date.issued2014-
dc.date.submitted2013-10-
dc.identifier.citationCarvalho P. P., Leonor I. B., Smith B. J., Dias I. R., Reis R. L., Gimble J. M., Gomes M. E. Undifferentiated human adipose-derived stromal/stem cells loaded onto wet-spun starch-polycaprolactone scaffolds enhance bone regeneration: Nude mice calvarial defect in vivo study, Journal of Biomedical Materials and Research - Part A, pp. [Epub ahead of print], doi:DOI: 10.1002/jbm.a.34983, 2013por
dc.identifier.issn1552-4965por
dc.identifier.urihttps://hdl.handle.net/1822/26924-
dc.description.abstractThe repair of large bony defects remains challenging in the clinical setting. Human adipose-derived stromal/ stem cells (hASCs) have been reported to differentiate along different cell lineages, including the osteogenic. The objective of the present study was to assess the bone regeneration potential of undifferentiated hASCs loaded in starchpolycaprolactone (SPCL) scaffolds, in a critical-sized nude mice calvarial defect. Human ASCs were isolated from lipoaspirate of five female donors, cryopreserved, and pooled together. Critical-sized (4 mm) calvarial defects were created in the parietal bone of adult male nude mice. Defects were either left empty, treated with an SPCL scaffold alone, or SPCL scaffold with human ASCs. Histological analysis and Micro-CT imaging of the retrieved implants were performed. Improved new bone deposition and osseointegration was observed in SPCL loaded with hASC engrafted calvarial defects as compared to control groups that showed little healing. Nondifferentiated human ASCs enhance ossification of nonhealing nude mice calvarial defects, and wet-spun SPCL confirmed its suitability for bone tissue engineering. This study supports the potential translation for ASC use in the treatment of human skeletal defects.por
dc.description.sponsorshipContract grant sponsor: Portuguese Foundation for Science and Technology (FCT); contract grant numbers: SFRH/BD/44128/2008; MIT/ECE/0047/2009Contract grant sponsor: COBRE; contract grant number: NIH-8 P20 GM103528Contract grant sponsor: NORC; contract grant number: NIH 1P30-DK072476por
dc.language.isoengpor
dc.publisherJohn Wiley and Sonspor
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F44128%2F2008/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/110812/PT-
dc.relationNIH-8 P20 GM103528-
dc.relationNIH 1P30-DK072476-
dc.rightsrestrictedAccesspor
dc.subjectAdipose-derived stem cellspor
dc.subjectBone regenerationpor
dc.subjectCalvarial defectpor
dc.subjectCritical size defectpor
dc.subjectSPCLpor
dc.titleUndifferentiated human adipose-derived stromal/stem cells loaded onto wet-spun starch-polycaprolactone scaffolds enhance bone regeneration : nude mice calvarial defect in vivo studypor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttp://onlinelibrary.wiley.com/doi/10.1002/jbm.a.34983/abstractpor
dc.commentshttp://www.3bs.uminho.pt/node/17674por
sdum.publicationstatuspublishedpor
oaire.citationStartPage1por
oaire.citationEndPage10por
oaire.citationIssue9por
oaire.citationTitleJournal of Biomedical Materials Research Part Apor
oaire.citationVolume102por
dc.date.updated2013-10-25T15:56:55Z-
dc.identifier.doi10.1002/jbm.a.34983-
dc.identifier.pmid24123913por
dc.subject.wosScience & Technologypor
sdum.journalJournal of Biomedical Materials Research: Part Apor
Aparece nas coleções:3B’s - Artigos em revistas/Papers in scientific journals


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